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Precision Health Database


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Family Health History

Last data update: Sep 22, 2023. (Total: 61629 Documents since 2012)
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Query Trace: all[original query]>>Reviews/Commentaries[Product Type]
Experts say Found’s story highlights the extraordinary complexity of the problem for pregnant people living with SCD – and the critical importance of receiving proper, specialized care as early as possible. This is especially true now that medical advances in care and disease-modifying therapies have helped many people living with SCD survive well through their reproductive years. For parents-to-be, that means awareness is key. Individuals with SCD are at higher risk than the general population for preeclampsia, as Found discovered; but those with preeclampsia can go on to develop a condition called eclampsia, which can lead to seizures and even coma. People with SCD are also at higher risk for sepsis and blood clots. And there are risks for the fetus, such as lower-than-normal growth in the womb, preterm delivery, and stillbirth.
K Miller, Self, September 2023
Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics study.
Harris T Bland et al. J Genet Couns 2023
Is Lipoprotein(a) Clinically Actionable with Today's Evidence? The Answer is Yes.
Gary S Ma et al. Curr Cardiol Rep 2023
Principles of Genetic Counseling in Inherited Heart Conditions.
Susan Christian et al. Card Electrophysiol Clin 2023 15(3) 229-239
Are You Up to Date on Your Preventive Care?
CDC, July 2023
Talking About Your Family History of Cancer
CDC, July 2023
Family history can help identify health risks, but many Latino people know little about theirs
L Medrano, American Heart News, June 2023
Genetic Risk Scores and Missing Heritability in Ovarian Cancer.
Yasaman Fatapour et al. Genes 2023 14(3)
Are population level familial risks and germline genetics meeting each other?
Kari Hemminki et al. Hereditary cancer in clinical practice 2023 21(1) 3
Expanding Family Health History to Include Family Medication History
SB Haga et al, J Per Med, Feb 2023
The Role of Genetic Testing in Patients with Heritable Thoracic Aortic Diseases.
Emanuele Monda et al. Diagnostics (Basel, Switzerland) 2023 13(4)
Sudden cardiac death in the young: An update for NPs.
Julianne Doucette et al. The Nurse practitioner 2023 48(3) 21-28
A Focused Clinical Review of Lynch Syndrome.
Demetra Georgiou et al. Cancer management and research 2023 1567-85
Willingness to Pay for Down Syndrome Screening: A systematics Review.
Shima Nikjoo et al. Medical journal of the Islamic Republic of Iran 2023 36149
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?
Clabout Thomas et al. Genes 2023 14(1)
FAMILIAL PANCREATIC CANCER.
Nero Lorenzo Del et al. Clinics and research in hepatology and gastroenterology 2023 102079
At What Age Should We Stop Colorectal Cancer Screening? When Is Enough, Enough?
Lieberman David et al. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2023 32(1) 6-8
Genetic testing women with newly diagnosed breast cancer: What criteria are the most predictive of a positive test?
Metcalfe Kelly A et al. Cancer medicine 2022
Increasing Use and Impact of Family Health History in Medically Underserved Populations: Work in Progress
G Wood et al, CDC Blog Post, December 20, 2022
Hypertrophic Cardiomyopathy (HCM) and Family Health History of Sudden Death
CDC, December 2022
Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD).
Sekine Akinari et al. Journal of clinical medicine 2022 11(21)
Advances and Applications of Polygenic Scores for Coronary Artery Disease.
Patel Aniruddh P et al. Annual review of medicine 2022
Approach Toward Germline Predisposition Syndromes in Patients with Hematologic Malignancies.
Atluri Himachandana et al. Current hematologic malignancy reports 2022
When It Comes to Breast Cancer, Sometimes It’s All in the Family
G Miller, CDC Cancer, Blog, October 2022
Genetic testing for patients at risk of hereditary breast and ovarian cancer.
DeTroye Alisha et al. JAAPA : official journal of the American Academy of Physician Assistants 2022 35(10) 48-52
Familial Pancreatic Cancer.
Saba Helena et al. Gastroenterology clinics of North America 2022 51(3) 561-575
The Evolving Paradigm of Germline Testing in Pancreatic Ductal Adenocarcinoma and Implications for Clinical Practice.
Mohindroo Chirayu et al. Surgical pathology clinics 2022 15(3) 491-502
Familial colorectal cancer.
Mangas-Sanjuan Carolina et al. Best practice & research. Clinical gastroenterology 2022 58-59101798
FHH Quick App Review: How Can a Quality Review Process Assist Primary Care Providers in Choosing a Family Health History App for Patient Care?
GM Wood et al, Genes, August 2022
Genetic counseling for prion disease: Updates and best practices.
Goldman Jill S et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
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